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Journal of Chinese Pharmaceutical Sciences

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Study of the interactions between compound S009 and the extracellular loops of CC chemokine receptor 4 by capillary zone electrophoresis

Lu Yang, Pazilaiti Yakufu, Meina Li, Xiaomei Ling*, Zhongjie Li, Ying Wang*   

  1. 1. State Key Laboratory of Natural and Biomimetic Drugs; Department of Pharmaceutical Analysis, School of Pharmaceutical Sciences, Peking University Health Science Center, Beijing 100191, China
    2. Center for Human Disease Genomics; Department of Medical Immunology, School of Basic Medical Sciences, Peking University Health Science Center, Beijing 100191, China
  • Received:2013-11-09 Revised:2013-12-01 Online:2014-03-13 Published:2013-12-23
  • Contact: *Corresponding author. Tel.: 86-10-82801590; 86-10-82802414; E-mail: lingxm@bjmu.edu.cn; yw@bjmu.edu.cn
  • About author:*Corresponding author. Tel.: 86-10-82801590; 86-10-82802414; E-mail: lingxm@bjmu.edu.cn; yw@bjmu.edu.cn
  • Supported by:
    National Natural Science Foundation (Grant No. 81072612, 31270915 and 81071749), Specialized Research Fund for the Doctoral Program of Higher Education of China (Grant No. 20110001110021 and 20120001110001) and the Open Foundation of State Key Laboratory of Natural and Biomimetic Drugs (Grant No. K20110109).

Abstract:

CC chemokine receptor 4 (CCR4) is a G-protein-coupled receptor which plays a pivotal role in allergic inflammation. In the present study, three extracellular loops (EL1−3) of CCR4 were synthesized, and the interactions between the extracellular loops and compound S009 were investigated using capillary zone electrophoresis (CZE). Both qualitative and quantitative characterizations of the compound-peptide binding were carried out. The experimental data indicated that compound S009 exhibited interactions with EL3, and a binding constant of (12.5±0.19)×104 M-1 was determined using the Scatchard plot. Our study identified the specific domains of CCR4 that could be targeted by small molecules and provided insights for the discovery of novel CCR4 antagonists. 

Key words: CCR4, CZE, Compound S009, ML40, Extracellular loops

CLC Number: 

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